TMEM237 transmembrane protein 237

Information
Symbol
TMEM237
Type
protein-coding
Description
transmembrane protein 237
Entrez Gene ID
65062
Genome
hg19
Position
chr2:202,484,909-202,508,226
Genome
hg38
Position
chr2:201,620,186-201,643,503
MIM
614423 OMIM
HGNC
HGNC:14432 HGNC
Ensembl
ENSG00000155755 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 50
Likely pathogenic 0 32
Benign 0 86
Likely benign 0 276
Conflicting classifications of pathogenicity 0 32
Uncertain significance 2 430
Ranking
ClinVar
0
0
124
718
4
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM ALS2CR4
SYNONYM JBTS14
MIM 614423 OMIM
HGNC HGNC:14432 HGNC
Ensembl ENSG00000155755 Ensembl
AllianceGenome HGNC:14432
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409883.7 hg38 chr2 201,620,186 201,643,503 23,318
ENST00000409444.6 hg38 chr2 201,620,184 201,642,944 22,761
ENST00000621467.5 hg38 chr2 201,620,200 201,642,670 22,471
ENST00000409444.6 hg19 chr2 202,484,907 202,507,667 22,761
ENST00000409883.7 hg19 chr2 202,484,909 202,508,226 23,318
ENST00000621467.5 hg19 chr2 202,484,923 202,507,393 22,471
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